The purpose of this study is to determine the surgical and clinical outcomes of patients receiving total knee replacement with the same implant using two different types of cutting guides during surgery: 1. Standard knee cutting guides; 2. MRI generated patient specific custom cutting guides. Both types of cutting guides used in this study are registered with the U.S. Food and Drug Administration (FDA) and are routinely used for knee replacement surgery. However, it is unknown if one type of cutting guide has risks or benefits over the other.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
25
Randomization to instrumentation to be used for primary total knee replacement; either standard knee cutting guides or MRI generated patient specific custom cutting guides.
Washington University
St Louis, Missouri, United States
Patient dissatisfaction following primary total knee replacement.
Time frame: Preoperatively, intraoperatively, and at four to six weeks, three months, six months, and one year postoperatively.
Postoperative recovery time following primary total knee replacement.
Time frame: Immediate postoperative period (prior to discharge) and at four to six weeks, three months, six months, and one year postoperatively.
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